Works matching DE "NIGHT blindness"
Results: 93
Phenotypic characterization of complete CSNB in the inbred research beagle: how common is CSNB in research and companion dogs?
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- Documenta Ophthalmologica, 2018, v. 137, n. 2, p. 87, doi. 10.1007/s10633-018-9653-y
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- Article
Riggs-type dominant congenital stationary night blindness: ERG findings, a new GNAT1 mutation and a systemic association.
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- Documenta Ophthalmologica, 2018, v. 137, n. 1, p. 57, doi. 10.1007/s10633-018-9651-0
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- Article
ISCEV extended protocol for the photopic On-Off ERG.
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- Documenta Ophthalmologica, 2018, v. 136, n. 3, p. 199, doi. 10.1007/s10633-018-9645-y
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- Publication type:
- Article
Phenotypic expansion and progression of <italic>SPATA7</italic>-associated retinitis pigmentosa.
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- 2018
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- Publication type:
- Case Study
Recurrent episodes of night blindness in a patient with short bowel syndrome.
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- Documenta Ophthalmologica, 2015, v. 131, n. 3, p. 221, doi. 10.1007/s10633-015-9516-8
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- Article
Reduced rod electroretinograms in carrier parents of two Japanese siblings with autosomal recessive retinitis pigmentosa associated with PDE6B gene mutations.
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- Documenta Ophthalmologica, 2015, v. 131, n. 1, p. 71, doi. 10.1007/s10633-015-9497-7
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- Publication type:
- Article
Electrophysiological and microperimetry changes in vitamin A deficiency retinopathy.
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- Documenta Ophthalmologica, 2015, v. 130, n. 3, p. 231, doi. 10.1007/s10633-015-9484-z
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- Article
Estimating ON and OFF contributions to the photopic hill: normative data and clinical applications.
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- Documenta Ophthalmologica, 2014, v. 129, n. 1, p. 9, doi. 10.1007/s10633-014-9446-x
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- Article
Editor's comment.
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- 2013
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- Publication type:
- Editorial
Xerophthalmia and acquired night blindness in a patient with a history of gastrointestinal neoplasia and normal serum vitamin A levels.
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- Documenta Ophthalmologica, 2013, v. 126, n. 2, p. 159, doi. 10.1007/s10633-012-9370-x
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- Publication type:
- Article
Negative electroretinograms in the pediatric and adult population.
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- Documenta Ophthalmologica, 2012, v. 124, n. 1, p. 41, doi. 10.1007/s10633-011-9301-2
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- Publication type:
- Article
Macular Neovascularization in a Patient with Pigmented Paravenous Chorioretinal Atrophy.
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- Türkiye Klinikleri Journal of Case Reports, 2023, v. 31, n. 2, p. 63, doi. 10.5336/caserep.2022-94394
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- Publication type:
- Article
Smart Night-Vision Glasses with AI and Sensor Technology for Night Blindness and Retinitis Pigmentosa.
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- International Journal of Advanced Computer Science & Applications, 2025, v. 16, n. 2, p. 962, doi. 10.14569/ijacsa.2025.0160295
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- Publication type:
- Article
A Novel Splice-Site Variant in CACNA1F Causes a Phenotype Synonymous with Åland Island Eye Disease and Incomplete Congenital Stationary Night Blindness.
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- Genes, 2021, v. 12, n. 2, p. 171, doi. 10.3390/genes12020171
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- Publication type:
- Article
Metabotropic glutamate receptor 6 signaling enhances TRPM1 calcium channel function and increases melanin content in human melanocytes.
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- Pigment Cell & Melanoma Research, 2013, v. 26, n. 3, p. 348, doi. 10.1111/pcmr.12083
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- Publication type:
- Article
Ocular Fundus Imaging for the Diagnosis of Progressive Retinal Atrophy - A Study in 31 Dogs.
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- Intas Polivet, 2016, v. 17, n. 2, p. 426
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- Publication type:
- Article
Utilizing Zebrafish Visual Behaviors in Drug Screening for Retinal Degeneration.
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- International Journal of Molecular Sciences, 2017, v. 18, n. 6, p. 1185, doi. 10.3390/ijms18061185
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- Publication type:
- Article
Network and Atomistic Simulations Unveil the Structural Determinants of Mutations Linked to Retinal Diseases.
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- PLoS Computational Biology, 2013, v. 9, n. 8, p. 1, doi. 10.1371/journal.pcbi.1003207
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- Publication type:
- Article
Genome-wide association study and whole-genome sequencing identify a deletion in LRIT3 associated with canine congenital stationary night blindness.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-50573-7
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- Publication type:
- Article
Extensive Macular Atrophy with Pseudodrusen Imaged with OCT Angiography.
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- 2018
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- Publication type:
- Case Study
Psychophysical measures of visual function and everyday perceptual experience in a case of congenital stationary night blindness.
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- Clinical Ophthalmology, 2016, v. 10, p. 1593, doi. 10.2147/OPTH.S99593
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- Publication type:
- Article
Infrared imaging enhances retinal crystals in Bietti's crystalline dystrophy.
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- 2015
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- Publication type:
- Case Study
Color vision abnormality as an initial presentation of the complete type of congenital stationary night blindness.
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- 2013
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- Publication type:
- Case Study
Electrophysiological findings in Oguchi disease.
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- 2013
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- Publication type:
- Case Study
RIM1/2-Mediated Facilitation of Cav1.4 Channel Opening Is Required for Ca<sup>2+</sup>-Stimulated Release in Mouse Rod Photoreceptors.
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- Journal of Neuroscience, 2015, v. 35, n. 38, p. 13133, doi. 10.1523/JNEUROSCI.0658-15.2015
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- Publication type:
- Article
GPR179 Is Required for High Sensitivity of the mGluR6 Signaling Cascade in Depolarizing Bipolar Cells.
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- Journal of Neuroscience, 2014, v. 34, n. 18, p. 6334, doi. 10.1523/JNEUROSCI.4044-13.2014
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- Publication type:
- Article
An association between subclinical familial exudative vitreoretinopathy and rod-cone dystrophy.
- Published in:
- 2014
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- Publication type:
- Case Study
Retinoids as chemopreventive agents.
- Published in:
- 2016
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- Publication type:
- journal article
Onchocerciasis as a Risk Factor for Night Blindness.
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- Ophthalmic Epidemiology, 2012, v. 19, n. 4, p. 204, doi. 10.3109/09286586.2012.680529
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- Publication type:
- Article
HLA-A29-positive Birdshot Chorioretinopathy in a Hispanic Patient.
- Published in:
- 2016
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- Publication type:
- Case Study
A Case Report of Vogt's Limbal Girdle and Retinitis Pigmentosa in a Thirteen-Year-Old Boy: A Rare and Unusual Association.
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- Case Reports in Ophthalmology, 2015, v. 6, n. 3, p. 311, doi. 10.1159/000439265
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- Publication type:
- Article
Multiple congenital ocular anomalies and the silver dapple gene.
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- Equine Veterinary Education, 2013, v. 25, n. 11, p. 556, doi. 10.1111/eve.12099
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- Publication type:
- Article
A maternally inherited 8.05 Mb Xq21 deletion associated with Choroideremia, deafness, and mental retardation syndrome in a male patient.
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- Molecular Cytogenetics (17558166), 2017, v. 10, p. 1, doi. 10.1186/s13039-017-0324-6
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- Publication type:
- Article
Outer retinal structural anomaly due to frameshift mutation in CACNA1F gene.
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- Eye, 2012, v. 26, n. 9, p. 1278, doi. 10.1038/eye.2012.125
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- Publication type:
- Article
I Cannot Read as Well...My Speech Is Slower and Writing Now Poor.
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- Journal of Pediatric Ophthalmology & Strabismus, 2017, v. 54, n. 3, p. 138, doi. 10.3928/01913913-20170412-01
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- Publication type:
- Article
Mizuo Nakamura Phenomenon.
- Published in:
- 2015
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- Publication type:
- Case Study
Black Dots and the Evil Eye!
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- 2015
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- Publication type:
- Case Study
Identification of a Novel Homozygous Nonsense Mutation Confirms the Implication of GNAT1 in Rod-Cone Dystrophy.
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- 2016
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- Publication type:
- Case Study
Congenital stationary night blindness with hypoplastic discs, negative electroretinogram and thinning of the inner nuclear layer.
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- Graefe's Archive of Clinical & Experimental Ophthalmology, 2016, v. 254, n. 10, p. 1951, doi. 10.1007/s00417-016-3346-6
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- Article
Determinants of gestational night blindness in pregnant women from Rio de Janeiro, Brazil.
- Published in:
- 2016
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- Publication type:
- journal article
Mutations in CERKL and RP1 cause retinitis pigmentosa in Pakistani families.
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- Human Genome Variation, 2020, v. 7, n. 1, p. 1, doi. 10.1038/s41439-020-0100-8
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- Publication type:
- Article
Novel gene mutation in a patient with Bietti crystalline dystrophy without corneal deposits.
- Published in:
- 2017
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- Publication type:
- Case Study
Next-generation sequencing confirms the implication of SLC24A1 in autosomal-recessive congenital stationary night blindness.
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- Clinical Genetics, 2016, v. 89, n. 6, p. 690, doi. 10.1111/cge.12746
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- Publication type:
- Article
Diagnóstico de la ceguera nocturna mediante entrevista normalizada y electrorretinografía.
- Published in:
- 2020
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- Publication type:
- journal article
Vitamin A deficiency is associated with body mass index and body adiposity in women with recommended intake of vitamin A.
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- 2018
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- Publication type:
- journal article
The use of handheld spectral domain optical coherence tomography in pediatric ophthalmology practice: Our experience of 975 infants and children.
- Published in:
- 2015
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- Publication type:
- journal article
Desferrioxamine-related ocular toxicity: A case report.
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- Indian Journal of Ophthalmology, 2012, v. 60, n. 4, p. 315, doi. 10.4103/0301-4738.98714
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- Publication type:
- Article
Night blindness, diet and health in Nepalese children: An ethno‐epidemiological investigation of local beliefs.
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- Ecology of Food & Nutrition, 2000, v. 39, n. 3, p. 199, doi. 10.1080/03670244.2000.9991615
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- Publication type:
- Article
Isotretinoin and night blindness.
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- Australasian Journal of Dermatology, 2014, v. 55, n. 3, p. 222, doi. 10.1111/ajd.12107
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- Publication type:
- Article
Clinical characteristics and disease progression of retinitis pigmentosa associated with PDE6B mutations in Korean patients.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-75902-z
- By:
- Publication type:
- Article